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4-MMPB (CAS 928853-86-5) is a small-molecule research compound that selectively inhibits 15-lipoxygenase and has been used in studies of cancer biology. It is provided as a high-purity research reagent with characterized activity and recommended storage conditions for long-term stability.
Selective 15-lipoxygenase inhibitor with reported IC50 ≈ 18 μM.
High purity suitable for research (≈98.5%).
Available in small pack sizes for laboratory use, including solid and solution formats.
Recommended storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years); in solvent at -80°C (up to 6 months) or -20°C (up to 1 month).
Molecular formula C16H19N5S and molecular weight 313.42, suitable for analytical characterization.
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4-MMPB is a small-molecule research compound that acts as a selective 15-lipoxygenase inhibitor and is provided for laboratory research use only. It has documented enzyme inhibition and cell viability data and is commonly used in biochemical assays and exploratory cellular studies.
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4-MMPB is a research reagent and selective 15-lipoxygenase inhibitor used in biochemical and pharmacological studies. Supplied as a solid with characterization data and supporting documents (COA, SDS), it is intended for research use only.
Solid, light yellow to orange appearance
Purity 98.5% (manufacturer reported)
Molecular weight 313.42 g/mol, formula C16H19N5S
Available in small milligram packages including 50 MG
Includes datasheet, certificate of analysis, and SDS for characterization and safety
Store powder at -20°C (3 years) or 4°C (2 years); in solvent store at -80°C or -20°C
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PR5-LL-CM01 is a potent protein arginine methyltransferase 5 (PRMT5) inhibitor with an IC50 of 7.5 μM. It exhibits anti-tumor activities and demonstrates efficacy in inhibiting cancer cells while showing low toxicity in normal cells.
Has IC50 values ranging from 2-4 μM in PDAC cells (PANC1, MiaPaCa2, and AsPC1) and 10-11 μM in CRC cells (HT29, HCT116, and DLD1).
Strongly inhibits colony-forming ability in both PANC1 and HT29 cells.
Inhibits NF-κB activation and its target gene expression in PDAC and CRC cells.
Significantly decreases TNFα and IL8 expression in both PANC1 and HT29 cells (at 0-15 μM).
Shows significant anti-tumor effects in PANC1 and HT29 xenografted mice in vivo (20 mg/kg; i.p.; 3 times per week) without visibly affecting their body weight.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More